A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14065



Internal ID15840544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32568705..32569948hg38UCSC Ensembl
Outerchr6:32568349..32572363hg38UCSC Ensembl
Innerchr6:32536482..32537725hg19UCSC Ensembl
Outerchr6:32536126..32540140hg19UCSC Ensembl
Innerchr6:32644460..32645703hg18UCSC Ensembl
Outerchr6:32644104..32648118hg18UCSC Ensembl
Innerchr6:32644460..32645703hg17UCSC Ensembl
Outerchr6:32644104..32648118hg17UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg384015
hg194015
hg184015
hg174015
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7883
Supporting Variants
SamplesNA18980
Known Genes
MethodOligo aCGH
AnalysisStatistical threshold = 5.0, minimum +/- log2 ratio = 0.25 and minimum number of probes = 2
PlatformAgilent-015686 Custom Human 244K CGH Microarray
Comments
ReferencePerry_et_al_2008
Pubmed ID18304495
Accession Number(s)nssv14065
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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